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Hydrochloric Acid → HCID 21471989, 화합물

HRID 1734076
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HRID 1734076 반응식
[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[CH:10]=[C:11]([CH2:13][CH2:14]Cl)[S:12][C:6]=2[CH2:5]1)(=[O:3])[CH3:2].Cl.[Cl:17][C:18]1[CH:19]=[CH:20][C:21]2[O:25][N:24]=[C:23]([CH:26]3[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]3)[C:22]=2[CH:32]=1.Cl>>[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[CH:10]=[C:11]([CH2:13][CH2:14][N:29]3[CH2:28][CH2:27][CH:26]([C:23]4[C:22]5[CH:32]=[C:18]([Cl:17])[CH:19]=[CH:20][C:21]=5[O:25][N:24]=4)[CH2:31][CH2:30]3)[S:12][C:6]=2[CH2:5]1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 214717815-Chloro-3-piperidin-4-yl-benzo[d]isoxazole hydrochlorideHCID 21472058HCID 21472058, 화합물

생성물 1

HCID 21471989HCID 21471989, 화합물수율 43.1%

실험 절차

The reaction and procedure were conducted in a similar manner as in Example 24 using 0.9 g of 6-acetyl-2-(2-chloroethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine and 1.0 g of 4-(5-chloro-1,2-benzisoxazol-3-yl)piperidine hydrochloride to give 0.7 g of 6-acetyl-2-(2-(4-(5-chloro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine as an oil, m.p. 122°-124° C. (decomposition) as a hydrochloride thereof.

후처리

  1. customThe reaction and procedure

출처 및 근거

ORD 기록
ord-5be703cff7b84aa0a6d49bc965aeb572
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05532240

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