HCID 15575170, compound → HCID 15575181, compound

HRID 1902251Notes

Reaction equation

HRID 1902251 reaction equation
[N:1]1([S:7]([C:10]2[CH:24]=[CH:23][C:13]3[S:14][C:15]4([C:21](=[O:22])[C:12]=3[CH:11]=2)[CH2:19][CH2:18]OC4=O)(=[O:9])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1>C(O)C>[N:1]1([S:7]([C:10]2[CH:24]=[CH:23][C:13]3[S:14][C:15]4([C:21](=[O:22])[C:12]=3[CH:11]=2)[CH2:19][CH2:18]4)(=[O:9])=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1

Participants

3

Procedure

5-Piperidinosulfonylspiro[benzo[b]thiophene-2(3H),1'-cyclopropan]-3-one was prepared by a similar procedure to that of Example 8 except for the use of 5-piperidinosulfonyl 4',5'-dihydrospiro[benzo[b]thiophene-2(3H),3'(2'H)-furan]-3,2'-dione obtained in Reference Example 17. Colorless prisms (from C2H5OH), mp 155.5°-157° C. Anal. Calcd. for C15H17NO3S: C, 55.70; H, 5.30; N, 4.33. Found: C, 55.74; H, 5.34; N, 4.50.

Workup

  1. customobtained in Reference Example 17

Sources & evidence

ORD record
ord-ea1197e0caed43f48eb942a3807ee9ee
Source dataset
uspto-grants-1982_12
Patent number
US04362740

Reaction notes

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