Sodium borohydride → HCID 178419093, 화합물

HRID 7165

반응식

HRID 7165 반응식
[CH3:1][C:2]1[NH:3][CH:4]=[C:5]([CH:7]=O)[N:6]=1.[NH2:9][CH2:10][C:11]1[CH:38]=[CH:37][C:14]([CH2:15][N:16]([CH2:27][C:28]2[NH:32][C:31]3[CH:33]=[CH:34][CH:35]=[CH:36][C:30]=3[N:29]=2)[CH:17]2[C:26]3[N:25]=[CH:24][CH:23]=[CH:22][C:21]=3[CH2:20][CH2:19][CH2:18]2)=[CH:13][CH:12]=1.[BH4-].[Na+]>CO>[NH:32]1[C:31]2[CH:33]=[CH:34][CH:35]=[CH:36][C:30]=2[N:29]=[C:28]1[CH2:27][N:16]([CH2:15][C:14]1[CH:13]=[CH:12][C:11]([CH2:10][NH:9][CH2:7][C:5]2[N:6]=[C:2]([CH3:1])[NH:3][CH:4]=2)=[CH:38][CH:37]=1)[CH:17]1[C:26]2[N:25]=[CH:24][CH:23]=[CH:22][C:21]=2[CH2:20][CH2:19][CH2:18]1

참가 물질

5

실험 절차

Using General Procedure B: A solution of 2-methyl-1H-imidazole-4-carbaldehyde (27.7 mg, 0.25 mmol) and (4-aminomethyl-benzyl)-(1H-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (100 mg, 0.25 mmol) in MeOH (2.0 mL) was stirred overnight at room temperature. NaBH4 (18.9 mg, 0.50 mmol) was added and the resultant mixture stirred for an additional 15 minutes. Purification of the crude yellow foam by column chromatography on silica gel (CH2Cl2/MeOH/NH4OH, 200:3:3) afforded the desired amine (65 mg, 53%) as a white foam.

후처리

  1. customPurification of the crude yellow foam by column chromatography on silica gel (CH2Cl2/MeOH/NH4OH, 200:3:3)

출처 및 근거

ORD 기록
ord-8ab4549260ae492c980f2cd8534f6614
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07084155B2

연결된 노트

불러오는 중…