ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Hydrochloric Acid → HCID 131711282、化合物

HRID 1764788
ノート
印刷プレビュー

反応式

HRID 1764788 の反応式
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:13]([NH:15][C@H:16]([C:32]([OH:34])=[O:33])[CH2:17][CH2:18][CH2:19][CH2:20][NH:21][C:22]([O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:23])=[O:14])[C@@H:3]([CH3:12])[O:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.Cl.[NH:43]([C:65]([O:67][C:68]([CH3:71])([CH3:70])[CH3:69])=[O:66])[C@H:44]([C:55]([O:57]N1C(=O)CCC1=O)=O)[C@@H:45]([CH3:54])[O:46][CH2:47][C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1.CCN(CC)CC>C1COCC1.CN(C=O)C.CCN(CC)CC.O.CCOC(C)=O.CC(O)=O>[NH:43]([C:65]([O:67][C:68]([CH3:69])([CH3:70])[CH3:71])=[O:66])[C@H:44]([C:55]([NH:1][C@H:2]([C:13]([NH:15][C@H:16]([C:32]([OH:34])=[O:33])[CH2:17][CH2:18][CH2:19][CH2:20][NH:21][C:22]([O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:23])=[O:14])[C@@H:3]([CH3:12])[O:4][CH2:5][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)=[O:57])[C@@H:45]([CH3:54])[O:46][CH2:47][C:48]1[CH:49]=[CH:50][CH:51]=[CH:52][CH:53]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

11

反応物 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 12879029Boc-Thr(Bzl)-OSuHCID 131711283HCID 131711283、化合物

生成物 1

HCID 131711282HCID 131711282、化合物

試薬・触媒・溶媒 6

HCID 8471Triethylamine触媒
HCID 176
Acetic Acid
溶媒
HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

Boc-Thr(Bzl)-Lys(Z)-OH (14.0 g, 24.5 mmol) was treated with 500 ml of 4.0 N HCl in THF for 30 minutes, evaporated to dryness, and re-evaporated twice with fresh THF. The oily residue solidified when treated with ether. The dried powder (11.4 g, 21.6 mmol) of the dipeptide hydrochloride salt was then dissolved in 140 ml DMF, cooled to 0°, and treated with Boc-Thr(Bzl)-OSu (8.8 g, 21.6 mmol) followed by 3.5 ml of Et3N. A few drops of Et3N was added to maintain a slightly basic condition while the mixture was stirred for an additional 24 hours at 25°. It was acidified with 5 ml of HOAc and then diluted with a large volume of water. The solid crude product precipitated was collected, dissolved in EtOAc, washed with H2O, dried over Na2SO4, and evaporated to dryness, leaving a glassy solid mass. Crystallized from EtOAc and petroleum ether: yield, 13.8 g (83.7%); mp 110°- 112°; [α]D25 = +19.45° (c 1, EtOAc).

後処理

  1. customevaporated to dryness
  2. customre-evaporated twice with fresh THF
  3. additiontreated with ether
  4. temperaturecooled to 0°
  5. temperatureto maintain a slightly basic condition while the mixture
  6. customThe solid crude product precipitated
  7. customwas collected
  8. dissolutiondissolved in EtOAc
  9. washwashed with H2O
  10. dry with materialdried over Na2SO4
  11. customevaporated to dryness
  12. customleaving a glassy solid mass
  13. customCrystallized from EtOAc and petroleum ether
  14. customyield

出典と根拠

ORDレコード
ord-874099034c7349b897219820e42ef54f
出典データセット
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04116951

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート