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Cyclopropanecarbonyl chloride → 2-Chloro-6-(cyclopropylcarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridine

HRID 2361644
ノート
印刷プレビュー

反応式

HRID 2361644 の反応式
Cl.[Cl:2][C:3]1[CH:12]=[CH:11][C:10]2[CH2:9][NH:8][CH2:7][CH2:6][C:5]=2[N:4]=1.CCN(C(C)C)C(C)C.[CH:22]1([C:25](Cl)=[O:26])[CH2:24][CH2:23]1>ClCCl.Cl>[Cl:2][C:3]1[CH:12]=[CH:11][C:10]2[CH2:9][N:8]([C:25]([CH:22]3[CH2:24][CH2:23]3)=[O:26])[CH2:7][CH2:6][C:5]=2[N:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 77637Cyclopropanecarbonyl chlorideHCID 81531DiisopropylethylamineHCID 184491652-Chloro-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride

生成物 1

HCID 582434152-Chloro-6-(cyclopropylcarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridine収率 105.6%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒
HCID 6344
Dichloromethane
溶媒
2 回

実験手順

To a room temperature stirred suspension of 2-chloro-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride (50 mg, 0.24 mmol) in dichloromethane (2 ml) under a nitrogen atmosphere was added DIPEA (0.12 ml, 0.73 mmol) followed by cyclopropyl carbonyl chloride (24 μl, 0.27 mmol). The resulting mixture was stirred for 16 hours, diluted with dichloromethane (30 ml) and 1M aq. HCl (2 ml). The organic layer was separated and washed with saturated aqueous NaHCO3 (15 ml) and brine (15 ml), dried (MgSO4), filtered and concentrated at reduced pressure to provide the title compound (60 mg, 95%) which was used without further purification.

後処理

  1. stirringThe resulting mixture was stirred for 16 hours
  2. customThe organic layer was separated
  3. washwashed with saturated aqueous NaHCO3 (15 ml) and brine (15 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated at reduced pressure

出典と根拠

ORDレコード
ord-0216f6721ccf4d0da782bd4c37e3b266
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08691804B2

反応ノート

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